Abstract
Henoch-Schönlein purpura (HSP) is a systemic vasculitis that is common in the pediatric population and often presents with the classical triad of palpable purpura, arthralgia, and abdominal pain. We describe a case of HSP in a 14-year-old adolescent girl who presented with atypical features of painful hemorrhagic bullae. The patient was treated with high-dose steroids, dapsone, and supportive therapy with remarkable improvement.
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CITATION STYLE
APA
Chen, C. B., Garlapati, S., Lancaster, J. D., Zinn, Z., Bacaj, P., & Patra, K. P. (2015). Bullous Henoch-Schönlein purpura in children. Cutis, 96(4), 248–252.
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